Canonical Allele Identifier: CA1339333465

Gene: AGXT

Linked Data

• dbSNP Id: rs1575709739

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240873826A>C , CM000664.2:g.240873826A>C	GRCh38
NC_000002.11:g.241813243A>C , CM000664.1:g.241813243A>C	GRCh37
NC_000002.10:g.241461916A>C	NCBI36
NG_008005.1:g.10082A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000307503.4:c.596-152A>C MANE Select	ENSP00000302620.3:n.596-152A>C
ENST00000307503.3:c.596-152A>C	ENSP00000302620.3:n.596-152A>C
ENST00000476698.1:n.332+777A>C
NM_000030.2:c.596-152A>C	NP_000021.1:n.596-152A>C
NM_000030.3:c.596-152A>C MANE Select	NP_000021.1:n.596-152A>C